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You searched for +publisher:"University of North Carolina" +contributor:("Nicewicz, David"). Showing records 1 – 19 of 19 total matches.

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University of North Carolina

1. Riener, Michelle. Synthesis of C2 Symmetric Cyclobutanes and gamma-Butyrolactones via Photoinduced Electron Transfer.

Degree: Chemistry, 2014, University of North Carolina

 Organic Photoredox Catalysis An overview of the principles of photoredox catalysis, alkene oxidation, and discussion of organic and inorganic photooxidants, applied in organic chemistry is… (more)

Subjects/Keywords: College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Riener, M. (2014). Synthesis of C2 Symmetric Cyclobutanes and gamma-Butyrolactones via Photoinduced Electron Transfer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:21b32235-2eec-4886-806a-00e3f46e9a8f

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Riener, Michelle. “Synthesis of C2 Symmetric Cyclobutanes and gamma-Butyrolactones via Photoinduced Electron Transfer.” 2014. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:21b32235-2eec-4886-806a-00e3f46e9a8f.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Riener, Michelle. “Synthesis of C2 Symmetric Cyclobutanes and gamma-Butyrolactones via Photoinduced Electron Transfer.” 2014. Web. 01 Dec 2020.

Vancouver:

Riener M. Synthesis of C2 Symmetric Cyclobutanes and gamma-Butyrolactones via Photoinduced Electron Transfer. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:21b32235-2eec-4886-806a-00e3f46e9a8f.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Riener M. Synthesis of C2 Symmetric Cyclobutanes and gamma-Butyrolactones via Photoinduced Electron Transfer. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:21b32235-2eec-4886-806a-00e3f46e9a8f

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

2. Nguyen, Tien Minh. Development of Two Organocatalytic Photoredox Transformations: The Enantioselective Cation Radical Diels-Alder Reaction and the Anti-Markovnikov Hydroamination of Alkenes.

Degree: Chemistry, 2014, University of North Carolina

 Herein we describe the development of two research projects within the field of organic photoredox catalysis. Both works involve the single electron oxidation of alkenes… (more)

Subjects/Keywords: College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Nguyen, T. M. (2014). Development of Two Organocatalytic Photoredox Transformations: The Enantioselective Cation Radical Diels-Alder Reaction and the Anti-Markovnikov Hydroamination of Alkenes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:8b80df4a-a4cb-4402-b9a0-ffcbf5c6ffa2

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Nguyen, Tien Minh. “Development of Two Organocatalytic Photoredox Transformations: The Enantioselective Cation Radical Diels-Alder Reaction and the Anti-Markovnikov Hydroamination of Alkenes.” 2014. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:8b80df4a-a4cb-4402-b9a0-ffcbf5c6ffa2.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Nguyen, Tien Minh. “Development of Two Organocatalytic Photoredox Transformations: The Enantioselective Cation Radical Diels-Alder Reaction and the Anti-Markovnikov Hydroamination of Alkenes.” 2014. Web. 01 Dec 2020.

Vancouver:

Nguyen TM. Development of Two Organocatalytic Photoredox Transformations: The Enantioselective Cation Radical Diels-Alder Reaction and the Anti-Markovnikov Hydroamination of Alkenes. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:8b80df4a-a4cb-4402-b9a0-ffcbf5c6ffa2.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Nguyen TM. Development of Two Organocatalytic Photoredox Transformations: The Enantioselective Cation Radical Diels-Alder Reaction and the Anti-Markovnikov Hydroamination of Alkenes. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:8b80df4a-a4cb-4402-b9a0-ffcbf5c6ffa2

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

3. Lee, Samuel. New Complexity-Building Reactions of α-Keto Esters.

Degree: Chemistry, 2017, University of North Carolina

 I. Introduction: Importance of Asymmetric Catalysis and the Reactivity Patterns of α-Keto Esters II. Synthesis of Complex Tertiary Glycolates by Enantioconvergent Arylation of Stereochemically Labile… (more)

Subjects/Keywords: College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Lee, S. (2017). New Complexity-Building Reactions of α-Keto Esters. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:7e9ef5d3-0d68-455a-98a4-5d27b67b7d4b

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lee, Samuel. “New Complexity-Building Reactions of α-Keto Esters.” 2017. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:7e9ef5d3-0d68-455a-98a4-5d27b67b7d4b.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lee, Samuel. “New Complexity-Building Reactions of α-Keto Esters.” 2017. Web. 01 Dec 2020.

Vancouver:

Lee S. New Complexity-Building Reactions of α-Keto Esters. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:7e9ef5d3-0d68-455a-98a4-5d27b67b7d4b.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lee S. New Complexity-Building Reactions of α-Keto Esters. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:7e9ef5d3-0d68-455a-98a4-5d27b67b7d4b

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

4. Beaver, Joshua. The Development of Receptors for Posttranslationally Modified Peptides in Water.

Degree: Chemistry, 2015, University of North Carolina

 The work presented in this dissertation highlights recent progress and advances in using dynamic combinatorial chemistry (DCC) for the investigation of molecular recognition in water.… (more)

Subjects/Keywords: Chemistry, Organic; Chemistry; Molecules; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Beaver, J. (2015). The Development of Receptors for Posttranslationally Modified Peptides in Water. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:07acc5c7-76bb-4b00-ba96-95e6f2af5811

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Beaver, Joshua. “The Development of Receptors for Posttranslationally Modified Peptides in Water.” 2015. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:07acc5c7-76bb-4b00-ba96-95e6f2af5811.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Beaver, Joshua. “The Development of Receptors for Posttranslationally Modified Peptides in Water.” 2015. Web. 01 Dec 2020.

Vancouver:

Beaver J. The Development of Receptors for Posttranslationally Modified Peptides in Water. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:07acc5c7-76bb-4b00-ba96-95e6f2af5811.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Beaver J. The Development of Receptors for Posttranslationally Modified Peptides in Water. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:07acc5c7-76bb-4b00-ba96-95e6f2af5811

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

5. Gesmundo, Nathan. The Development of Complexity Generating Organic Photoredox Transformations and the Application of These Transformations in Complex Molecule Synthesis.

Degree: Chemistry, 2015, University of North Carolina

 Described herein are three methods for the direct functionalization of alkenes, enabled by organic photoredox catalysis. Additionally, a model system studying the application of a… (more)

Subjects/Keywords: Chemistry, Organic; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Gesmundo, N. (2015). The Development of Complexity Generating Organic Photoredox Transformations and the Application of These Transformations in Complex Molecule Synthesis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:3eb42de0-b8bc-449f-a83e-b9a07eb3ea78

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gesmundo, Nathan. “The Development of Complexity Generating Organic Photoredox Transformations and the Application of These Transformations in Complex Molecule Synthesis.” 2015. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:3eb42de0-b8bc-449f-a83e-b9a07eb3ea78.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gesmundo, Nathan. “The Development of Complexity Generating Organic Photoredox Transformations and the Application of These Transformations in Complex Molecule Synthesis.” 2015. Web. 01 Dec 2020.

Vancouver:

Gesmundo N. The Development of Complexity Generating Organic Photoredox Transformations and the Application of These Transformations in Complex Molecule Synthesis. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:3eb42de0-b8bc-449f-a83e-b9a07eb3ea78.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gesmundo N. The Development of Complexity Generating Organic Photoredox Transformations and the Application of These Transformations in Complex Molecule Synthesis. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:3eb42de0-b8bc-449f-a83e-b9a07eb3ea78

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

6. Jackson, Anne-Martine. UTILIZING FUNCTIONALIZATION TO ACCESS ADVANCED MATERIALS PROPERTIES.

Degree: Chemistry, 2015, University of North Carolina

 While there are many materials that can perform a single selected task very well, there is a growing need for smart materials to advance technology… (more)

Subjects/Keywords: Chemistry; Polymers; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Jackson, A. (2015). UTILIZING FUNCTIONALIZATION TO ACCESS ADVANCED MATERIALS PROPERTIES. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:5770de30-cf9a-46ff-8663-1bebf60900cb

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jackson, Anne-Martine. “UTILIZING FUNCTIONALIZATION TO ACCESS ADVANCED MATERIALS PROPERTIES.” 2015. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:5770de30-cf9a-46ff-8663-1bebf60900cb.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jackson, Anne-Martine. “UTILIZING FUNCTIONALIZATION TO ACCESS ADVANCED MATERIALS PROPERTIES.” 2015. Web. 01 Dec 2020.

Vancouver:

Jackson A. UTILIZING FUNCTIONALIZATION TO ACCESS ADVANCED MATERIALS PROPERTIES. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:5770de30-cf9a-46ff-8663-1bebf60900cb.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Jackson A. UTILIZING FUNCTIONALIZATION TO ACCESS ADVANCED MATERIALS PROPERTIES. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:5770de30-cf9a-46ff-8663-1bebf60900cb

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

7. Krabbe, Scott. Strategic Applications of New Redox Transformations in Organic Synthesis.

Degree: Chemistry, 2015, University of North Carolina

 The dissertation contains three distinct parts. Part A: Aerobic hydroperoxidation of Meldrum's acid derivatives via a Cu(II)-catalyzed process is presented. The mild reaction conditions are… (more)

Subjects/Keywords: Chemistry; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Krabbe, S. (2015). Strategic Applications of New Redox Transformations in Organic Synthesis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:33d59dd0-3039-4c1b-9624-4e925e857254

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Krabbe, Scott. “Strategic Applications of New Redox Transformations in Organic Synthesis.” 2015. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:33d59dd0-3039-4c1b-9624-4e925e857254.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Krabbe, Scott. “Strategic Applications of New Redox Transformations in Organic Synthesis.” 2015. Web. 01 Dec 2020.

Vancouver:

Krabbe S. Strategic Applications of New Redox Transformations in Organic Synthesis. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:33d59dd0-3039-4c1b-9624-4e925e857254.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Krabbe S. Strategic Applications of New Redox Transformations in Organic Synthesis. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:33d59dd0-3039-4c1b-9624-4e925e857254

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

8. Li, Wentao. Fundamental Understanding of a High Performance Polymer for Organic Photovoltaics and New Material Development by Rational Molecular Engineering.

Degree: Chemistry, 2015, University of North Carolina

 Organic photovoltaics are a promising renewable energy technology. Development of novel materials and device architecture for further enhancing their efficiency requires fundamental understanding of the… (more)

Subjects/Keywords: Polymers; Materials science; Chemistry, Organic; Chemistry; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Li, W. (2015). Fundamental Understanding of a High Performance Polymer for Organic Photovoltaics and New Material Development by Rational Molecular Engineering. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:a487ff37-f8c4-4a0a-8d35-9f62436dad20

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Li, Wentao. “Fundamental Understanding of a High Performance Polymer for Organic Photovoltaics and New Material Development by Rational Molecular Engineering.” 2015. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:a487ff37-f8c4-4a0a-8d35-9f62436dad20.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Li, Wentao. “Fundamental Understanding of a High Performance Polymer for Organic Photovoltaics and New Material Development by Rational Molecular Engineering.” 2015. Web. 01 Dec 2020.

Vancouver:

Li W. Fundamental Understanding of a High Performance Polymer for Organic Photovoltaics and New Material Development by Rational Molecular Engineering. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:a487ff37-f8c4-4a0a-8d35-9f62436dad20.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Li W. Fundamental Understanding of a High Performance Polymer for Organic Photovoltaics and New Material Development by Rational Molecular Engineering. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:a487ff37-f8c4-4a0a-8d35-9f62436dad20

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

9. Morse, Peter. THE DEVELOPMENT OF AN ENANTIOSELECTIVE CATION RADICAL DIELS-ALDER REACTION AND OTHER COMPLEXITY GENERATING TRANSFORMATIONS.

Degree: Chemistry, 2015, University of North Carolina

 Herein is described the development of three synthetic transformations that are united in their being initiated by the single electron oxidation of olefins to cation… (more)

Subjects/Keywords: Chemistry; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Morse, P. (2015). THE DEVELOPMENT OF AN ENANTIOSELECTIVE CATION RADICAL DIELS-ALDER REACTION AND OTHER COMPLEXITY GENERATING TRANSFORMATIONS. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:6389429e-627c-4fc4-93a6-edcf3c8fad22

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Morse, Peter. “THE DEVELOPMENT OF AN ENANTIOSELECTIVE CATION RADICAL DIELS-ALDER REACTION AND OTHER COMPLEXITY GENERATING TRANSFORMATIONS.” 2015. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:6389429e-627c-4fc4-93a6-edcf3c8fad22.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Morse, Peter. “THE DEVELOPMENT OF AN ENANTIOSELECTIVE CATION RADICAL DIELS-ALDER REACTION AND OTHER COMPLEXITY GENERATING TRANSFORMATIONS.” 2015. Web. 01 Dec 2020.

Vancouver:

Morse P. THE DEVELOPMENT OF AN ENANTIOSELECTIVE CATION RADICAL DIELS-ALDER REACTION AND OTHER COMPLEXITY GENERATING TRANSFORMATIONS. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:6389429e-627c-4fc4-93a6-edcf3c8fad22.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Morse P. THE DEVELOPMENT OF AN ENANTIOSELECTIVE CATION RADICAL DIELS-ALDER REACTION AND OTHER COMPLEXITY GENERATING TRANSFORMATIONS. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:6389429e-627c-4fc4-93a6-edcf3c8fad22

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

10. Horwitz, Matthew. Complexity-building Transformations Enabled by Brønsted Base Organocatalysis and Progress Toward the Total Synthesis of the Veratrum Alkaloids Jervine, Cyclopamine, and Veratramine.

Degree: Chemistry, 2017, University of North Carolina

 I. Asymmetric Organocatalytic Reductive Coupling Reactions between Isatins and Aldehydes A fully organic phosphite-mediated stereoselective reductive coupling reaction between isatins and aldehydes was developed. A… (more)

Subjects/Keywords: College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Horwitz, M. (2017). Complexity-building Transformations Enabled by Brønsted Base Organocatalysis and Progress Toward the Total Synthesis of the Veratrum Alkaloids Jervine, Cyclopamine, and Veratramine. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:50b0474c-66d3-4f55-841d-1531e5972072

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Horwitz, Matthew. “Complexity-building Transformations Enabled by Brønsted Base Organocatalysis and Progress Toward the Total Synthesis of the Veratrum Alkaloids Jervine, Cyclopamine, and Veratramine.” 2017. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:50b0474c-66d3-4f55-841d-1531e5972072.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Horwitz, Matthew. “Complexity-building Transformations Enabled by Brønsted Base Organocatalysis and Progress Toward the Total Synthesis of the Veratrum Alkaloids Jervine, Cyclopamine, and Veratramine.” 2017. Web. 01 Dec 2020.

Vancouver:

Horwitz M. Complexity-building Transformations Enabled by Brønsted Base Organocatalysis and Progress Toward the Total Synthesis of the Veratrum Alkaloids Jervine, Cyclopamine, and Veratramine. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:50b0474c-66d3-4f55-841d-1531e5972072.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Horwitz M. Complexity-building Transformations Enabled by Brønsted Base Organocatalysis and Progress Toward the Total Synthesis of the Veratrum Alkaloids Jervine, Cyclopamine, and Veratramine. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:50b0474c-66d3-4f55-841d-1531e5972072

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

11. Cavanaugh, Cortney. APPLICATIONS OF ORGANIC PHOTOREDOX CATALYSIS IN THE DEVELOPMENT OF ALKENE FUNCTIONALIZATION METHODS TOWARD THE SYNTHESIS OF α–BENZYLOXYAMINO- AND HALO-LACTONES.

Degree: Chemistry, 2018, University of North Carolina

 I. Introduction To Organic Photoredox Catalysis An overview of the photophysical and electrochemical components of organic photoredox catalysis and its applications in alkene functionalization reactions… (more)

Subjects/Keywords: College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Cavanaugh, C. (2018). APPLICATIONS OF ORGANIC PHOTOREDOX CATALYSIS IN THE DEVELOPMENT OF ALKENE FUNCTIONALIZATION METHODS TOWARD THE SYNTHESIS OF α–BENZYLOXYAMINO- AND HALO-LACTONES. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:c0e9aba7-5743-4afa-8692-8e96674f5ef2

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Cavanaugh, Cortney. “APPLICATIONS OF ORGANIC PHOTOREDOX CATALYSIS IN THE DEVELOPMENT OF ALKENE FUNCTIONALIZATION METHODS TOWARD THE SYNTHESIS OF α–BENZYLOXYAMINO- AND HALO-LACTONES.” 2018. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:c0e9aba7-5743-4afa-8692-8e96674f5ef2.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Cavanaugh, Cortney. “APPLICATIONS OF ORGANIC PHOTOREDOX CATALYSIS IN THE DEVELOPMENT OF ALKENE FUNCTIONALIZATION METHODS TOWARD THE SYNTHESIS OF α–BENZYLOXYAMINO- AND HALO-LACTONES.” 2018. Web. 01 Dec 2020.

Vancouver:

Cavanaugh C. APPLICATIONS OF ORGANIC PHOTOREDOX CATALYSIS IN THE DEVELOPMENT OF ALKENE FUNCTIONALIZATION METHODS TOWARD THE SYNTHESIS OF α–BENZYLOXYAMINO- AND HALO-LACTONES. [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:c0e9aba7-5743-4afa-8692-8e96674f5ef2.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Cavanaugh C. APPLICATIONS OF ORGANIC PHOTOREDOX CATALYSIS IN THE DEVELOPMENT OF ALKENE FUNCTIONALIZATION METHODS TOWARD THE SYNTHESIS OF α–BENZYLOXYAMINO- AND HALO-LACTONES. [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:c0e9aba7-5743-4afa-8692-8e96674f5ef2

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

12. Grandjean, Jean-Marc. Anti-Markovnikov Hydrofluorination, Hydrooxysulfonylation and Hydration of Styrenes - Photoredox catalytic Polar-Radical Crossover Cycloaddition of Olefins and Allylic Nucleophiles.

Degree: Chemistry, 2014, University of North Carolina

 Described herein are two general methodologies for the direct functionalization of Olefins. The direct addition of hydrogen fluoride across a carbon-carbon double bond was enabled… (more)

Subjects/Keywords: College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Grandjean, J. (2014). Anti-Markovnikov Hydrofluorination, Hydrooxysulfonylation and Hydration of Styrenes - Photoredox catalytic Polar-Radical Crossover Cycloaddition of Olefins and Allylic Nucleophiles. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e68364d5-e1e0-40bc-a09d-dde1b6eb3225

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Grandjean, Jean-Marc. “Anti-Markovnikov Hydrofluorination, Hydrooxysulfonylation and Hydration of Styrenes - Photoredox catalytic Polar-Radical Crossover Cycloaddition of Olefins and Allylic Nucleophiles.” 2014. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:e68364d5-e1e0-40bc-a09d-dde1b6eb3225.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Grandjean, Jean-Marc. “Anti-Markovnikov Hydrofluorination, Hydrooxysulfonylation and Hydration of Styrenes - Photoredox catalytic Polar-Radical Crossover Cycloaddition of Olefins and Allylic Nucleophiles.” 2014. Web. 01 Dec 2020.

Vancouver:

Grandjean J. Anti-Markovnikov Hydrofluorination, Hydrooxysulfonylation and Hydration of Styrenes - Photoredox catalytic Polar-Radical Crossover Cycloaddition of Olefins and Allylic Nucleophiles. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:e68364d5-e1e0-40bc-a09d-dde1b6eb3225.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Grandjean J. Anti-Markovnikov Hydrofluorination, Hydrooxysulfonylation and Hydration of Styrenes - Photoredox catalytic Polar-Radical Crossover Cycloaddition of Olefins and Allylic Nucleophiles. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:e68364d5-e1e0-40bc-a09d-dde1b6eb3225

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

13. Hamilton, David. Anti-Markovnikov Addition Reactions of Oxy-Acids to Alkenes Enabled by Photoredox Catalysis.

Degree: Chemistry, 2014, University of North Carolina

 The addition of nucleophiles to alkenes with complete anti-Markovnikov selectivity employing reagents in catalytic quantities has been a major challenge for the field of organic… (more)

Subjects/Keywords: Chemistry, Organic; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Hamilton, D. (2014). Anti-Markovnikov Addition Reactions of Oxy-Acids to Alkenes Enabled by Photoredox Catalysis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:bd86f2be-9701-4ae0-9cf3-bc65e88f04d4

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hamilton, David. “Anti-Markovnikov Addition Reactions of Oxy-Acids to Alkenes Enabled by Photoredox Catalysis.” 2014. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:bd86f2be-9701-4ae0-9cf3-bc65e88f04d4.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hamilton, David. “Anti-Markovnikov Addition Reactions of Oxy-Acids to Alkenes Enabled by Photoredox Catalysis.” 2014. Web. 01 Dec 2020.

Vancouver:

Hamilton D. Anti-Markovnikov Addition Reactions of Oxy-Acids to Alkenes Enabled by Photoredox Catalysis. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:bd86f2be-9701-4ae0-9cf3-bc65e88f04d4.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hamilton D. Anti-Markovnikov Addition Reactions of Oxy-Acids to Alkenes Enabled by Photoredox Catalysis. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:bd86f2be-9701-4ae0-9cf3-bc65e88f04d4

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

14. Perkowski, Andrew. Direct, Catalytic, Intermolecular Anti-Markovnikov Hydroacetoxylations of Alkenes Enabled via Photoredox Catalysis, and Investigations into the Mechanism of the Polymerization of 4-Methoxystyrene Initiated by Pyrylium Salts.

Degree: Chemistry, 2014, University of North Carolina

 I. Intermolecular Anti-Markovnikov Addition of Oxygen Nucleophiles to Alkenes: Direct and Indirect Catalytic Methods to Address a Fundamental Challenge Markovnikov versus anti-Markovnikov functionalization of alkenes… (more)

Subjects/Keywords: Chemistry; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Perkowski, A. (2014). Direct, Catalytic, Intermolecular Anti-Markovnikov Hydroacetoxylations of Alkenes Enabled via Photoredox Catalysis, and Investigations into the Mechanism of the Polymerization of 4-Methoxystyrene Initiated by Pyrylium Salts. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b736f122-ce43-4e96-b937-c8828559ad4d

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Perkowski, Andrew. “Direct, Catalytic, Intermolecular Anti-Markovnikov Hydroacetoxylations of Alkenes Enabled via Photoredox Catalysis, and Investigations into the Mechanism of the Polymerization of 4-Methoxystyrene Initiated by Pyrylium Salts.” 2014. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:b736f122-ce43-4e96-b937-c8828559ad4d.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Perkowski, Andrew. “Direct, Catalytic, Intermolecular Anti-Markovnikov Hydroacetoxylations of Alkenes Enabled via Photoredox Catalysis, and Investigations into the Mechanism of the Polymerization of 4-Methoxystyrene Initiated by Pyrylium Salts.” 2014. Web. 01 Dec 2020.

Vancouver:

Perkowski A. Direct, Catalytic, Intermolecular Anti-Markovnikov Hydroacetoxylations of Alkenes Enabled via Photoredox Catalysis, and Investigations into the Mechanism of the Polymerization of 4-Methoxystyrene Initiated by Pyrylium Salts. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:b736f122-ce43-4e96-b937-c8828559ad4d.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Perkowski A. Direct, Catalytic, Intermolecular Anti-Markovnikov Hydroacetoxylations of Alkenes Enabled via Photoredox Catalysis, and Investigations into the Mechanism of the Polymerization of 4-Methoxystyrene Initiated by Pyrylium Salts. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:b736f122-ce43-4e96-b937-c8828559ad4d

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

15. Zeller, Mary. Application of Organic Photoredox Catalysis in New Reaction Methodology: Synthesis of Butyrolactones via Polar Radical Crossover Cycloaddition and Hydrodecarboxylation of Carboxylic Acids.

Degree: Chemistry, 2016, University of North Carolina

 Synthesis of Butyrolactones via Polar Radical Crossover Cycloaddition A direct catalytic synthesis of γ-butyrolactones from simple alkene and unsaturated acid starting materials is reported. The… (more)

Subjects/Keywords: College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Zeller, M. (2016). Application of Organic Photoredox Catalysis in New Reaction Methodology: Synthesis of Butyrolactones via Polar Radical Crossover Cycloaddition and Hydrodecarboxylation of Carboxylic Acids. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e9843dd7-c490-44c1-abba-5af0465789dd

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zeller, Mary. “Application of Organic Photoredox Catalysis in New Reaction Methodology: Synthesis of Butyrolactones via Polar Radical Crossover Cycloaddition and Hydrodecarboxylation of Carboxylic Acids.” 2016. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:e9843dd7-c490-44c1-abba-5af0465789dd.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zeller, Mary. “Application of Organic Photoredox Catalysis in New Reaction Methodology: Synthesis of Butyrolactones via Polar Radical Crossover Cycloaddition and Hydrodecarboxylation of Carboxylic Acids.” 2016. Web. 01 Dec 2020.

Vancouver:

Zeller M. Application of Organic Photoredox Catalysis in New Reaction Methodology: Synthesis of Butyrolactones via Polar Radical Crossover Cycloaddition and Hydrodecarboxylation of Carboxylic Acids. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:e9843dd7-c490-44c1-abba-5af0465789dd.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zeller M. Application of Organic Photoredox Catalysis in New Reaction Methodology: Synthesis of Butyrolactones via Polar Radical Crossover Cycloaddition and Hydrodecarboxylation of Carboxylic Acids. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:e9843dd7-c490-44c1-abba-5af0465789dd

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

16. Geier, Michael. New Mechanisms for Turnover and Functionalization in the Platinum Initiated Cyclization of Polyenes.

Degree: Chemistry, 2014, University of North Carolina

 The replication of nature's ability to convert acyclic polyenes to polycycles has long been the target of synthetic chemists. Progress has been made through manipulation… (more)

Subjects/Keywords: Chemistry; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Geier, M. (2014). New Mechanisms for Turnover and Functionalization in the Platinum Initiated Cyclization of Polyenes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:992bb1a7-a59f-431a-af6c-acf4385da735

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Geier, Michael. “New Mechanisms for Turnover and Functionalization in the Platinum Initiated Cyclization of Polyenes.” 2014. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:992bb1a7-a59f-431a-af6c-acf4385da735.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Geier, Michael. “New Mechanisms for Turnover and Functionalization in the Platinum Initiated Cyclization of Polyenes.” 2014. Web. 01 Dec 2020.

Vancouver:

Geier M. New Mechanisms for Turnover and Functionalization in the Platinum Initiated Cyclization of Polyenes. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:992bb1a7-a59f-431a-af6c-acf4385da735.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Geier M. New Mechanisms for Turnover and Functionalization in the Platinum Initiated Cyclization of Polyenes. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:992bb1a7-a59f-431a-af6c-acf4385da735

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

17. Do, Dung. STEREOSELECTIVE FUNCTIONALIZATION OF MELDRUM'S ACIDS AND THE EFFORTS TOWARD TOTAL SYNTHESIS OF ECHINOSPORIN.

Degree: Chemistry, 2014, University of North Carolina

 I. Cu(II)-Catalyzed Aerobic Hydroperoxidation of Meldrum's Acid Derivatives and Application in Intramolecular Functionalization to Access Complex Building Blocks Aerobic hydroperoxidation of Meldrum's acid derivatives via… (more)

Subjects/Keywords: Chemistry; Chemistry, Organic; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Do, D. (2014). STEREOSELECTIVE FUNCTIONALIZATION OF MELDRUM'S ACIDS AND THE EFFORTS TOWARD TOTAL SYNTHESIS OF ECHINOSPORIN. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4fce5301-7cb1-4cfc-8b0a-8d5d6615a1c8

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Do, Dung. “STEREOSELECTIVE FUNCTIONALIZATION OF MELDRUM'S ACIDS AND THE EFFORTS TOWARD TOTAL SYNTHESIS OF ECHINOSPORIN.” 2014. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:4fce5301-7cb1-4cfc-8b0a-8d5d6615a1c8.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Do, Dung. “STEREOSELECTIVE FUNCTIONALIZATION OF MELDRUM'S ACIDS AND THE EFFORTS TOWARD TOTAL SYNTHESIS OF ECHINOSPORIN.” 2014. Web. 01 Dec 2020.

Vancouver:

Do D. STEREOSELECTIVE FUNCTIONALIZATION OF MELDRUM'S ACIDS AND THE EFFORTS TOWARD TOTAL SYNTHESIS OF ECHINOSPORIN. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:4fce5301-7cb1-4cfc-8b0a-8d5d6615a1c8.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Do D. STEREOSELECTIVE FUNCTIONALIZATION OF MELDRUM'S ACIDS AND THE EFFORTS TOWARD TOTAL SYNTHESIS OF ECHINOSPORIN. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:4fce5301-7cb1-4cfc-8b0a-8d5d6615a1c8

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

18. Giglio, Benjamin. Alkene Difunctionalization using Hydroxamic Acids.

Degree: Chemistry, 2014, University of North Carolina

 Alkene difunctionalizations are a core transformation in synthetic organic chemistry. A majority of these reactions proceed through polar or transition-metal-catalyzed methods. Alkene difunctionalizations that pass… (more)

Subjects/Keywords: Chemistry; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Giglio, B. (2014). Alkene Difunctionalization using Hydroxamic Acids. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:f02390e7-57bf-4363-b2c9-bdd3f9a81f5b

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Giglio, Benjamin. “Alkene Difunctionalization using Hydroxamic Acids.” 2014. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:f02390e7-57bf-4363-b2c9-bdd3f9a81f5b.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Giglio, Benjamin. “Alkene Difunctionalization using Hydroxamic Acids.” 2014. Web. 01 Dec 2020.

Vancouver:

Giglio B. Alkene Difunctionalization using Hydroxamic Acids. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:f02390e7-57bf-4363-b2c9-bdd3f9a81f5b.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Giglio B. Alkene Difunctionalization using Hydroxamic Acids. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:f02390e7-57bf-4363-b2c9-bdd3f9a81f5b

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Carolina

19. Nicewicz, David Andrew. The [1,2]-Brook rearrangement: novel carbon-carbon bond forming reactions and application to the total synthesis of zaragozic acid C.

Degree: Chemistry, 2006, University of North Carolina

 I. Catalytic Cyanation/Brook Rearrangement/C-Acylation Reactions of Acylsilanes A tandem nucleophile-catalyzed cyanation/Brook rearrangement/C-acylation has been developed. Phase transfer cocatalysts facilitate cyanide-catalyzed reactions between acylsilanes and cyanoformates… (more)

Subjects/Keywords: College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Nicewicz, D. A. (2006). The [1,2]-Brook rearrangement: novel carbon-carbon bond forming reactions and application to the total synthesis of zaragozic acid C. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:8c7e7756-1fc1-4c05-b62c-561d25caa5b7

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Nicewicz, David Andrew. “The [1,2]-Brook rearrangement: novel carbon-carbon bond forming reactions and application to the total synthesis of zaragozic acid C.” 2006. Thesis, University of North Carolina. Accessed December 01, 2020. https://cdr.lib.unc.edu/record/uuid:8c7e7756-1fc1-4c05-b62c-561d25caa5b7.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Nicewicz, David Andrew. “The [1,2]-Brook rearrangement: novel carbon-carbon bond forming reactions and application to the total synthesis of zaragozic acid C.” 2006. Web. 01 Dec 2020.

Vancouver:

Nicewicz DA. The [1,2]-Brook rearrangement: novel carbon-carbon bond forming reactions and application to the total synthesis of zaragozic acid C. [Internet] [Thesis]. University of North Carolina; 2006. [cited 2020 Dec 01]. Available from: https://cdr.lib.unc.edu/record/uuid:8c7e7756-1fc1-4c05-b62c-561d25caa5b7.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Nicewicz DA. The [1,2]-Brook rearrangement: novel carbon-carbon bond forming reactions and application to the total synthesis of zaragozic acid C. [Thesis]. University of North Carolina; 2006. Available from: https://cdr.lib.unc.edu/record/uuid:8c7e7756-1fc1-4c05-b62c-561d25caa5b7

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

.